DrugBank

MARCH 22, 2024

Self-Hosting: These ontologies and datasets are often downloadable and can be used within your own servers, providing a high level of control over security and infrastructure. Paid Knowledge Bases Paying for access or licensing a knowledge base can be a difficult decision to make.

Licensing 98

Licensing Licensing Research Clinical Trials 98

Perficient: Drug Development

JUNE 12, 2024

It is licensed for commercial use and open source) and is available in three models: CodeLlama, CodeLlama Python and CodeLlama Instruct. To install Ollama on your PC, you will first need to download the installer from the official Ollama website ( [link] ). Each model was released in three sizes with 7B, 13B, and 34B.

Production 52

Production Licensing Licensing Research 52

Drug Channels

SEPTEMBER 12, 2023

Those who preorder will receive a download link before October 10. CLICK HERE to download a free pre-publication overview (including key industry trends, the Table of Contents, and a List of Exhibits) You can pay online with all major credit cards (Visa, MasterCard, American Express, and Discover) or via PayPal.

Pharmaceuticals 40

Pharmaceuticals Pharmacy Biosimilars Licensing 40

The Pharma Data

NOVEMBER 23, 2020

View original content to download multimedia: [link]. . SOURCE Synthetic Biologics, Inc. . Source link.

Compliance 52

Compliance Licensing Licensing Clinical Trials 52

Perficient: Drug Development

JUNE 15, 2023

New test automation technologies are entering the market as the scope expands. The market was previously dominated by proprietary tools like selenium. However, new open-source tools are now leading the market. Playwright is one of many Test Automation Frameworks available in the market. What is Playwright? The Apache 2.0

Marketing 52

Marketing Licensing Licensing Engineering 52

The Pharma Data

NOVEMBER 1, 2020

In addition, Corlieve has licensed REGENXBIO’s NAV AAV9 technology for the TLE program. About IDinvest Idinvest Partners is a leading European mid-market private equity firm. View original content to download multimedia: [link]. Maryland , US), a leading gene therapy company. SOURCE Corlieve Therapeutics.

Therapies 52

Therapies Science Treatment Disease 52

The Pharma Data

DECEMBER 15, 2020

This is an important step towards a licensing agreement for Lipidor drug candidates, AKP01 and AKP02, for the treatment of psoriasis. This disclosure contains information that Lipidor is obliged to make public pursuant to the EU Market Abuse Regulation (EU nr 596/2014). Aurena Laboratories has already met the requirements of the U.S.

Production 52

Production Laboratories Licensing Licensing 52

The Premier Consulting Blog

MAY 14, 2023

All clinical trial or marketing applications submitted to the FDA must include a form that summarizes the content of the submission and any relevant information on the sponsor and drug for the reviewers. Q: When I try to download the form, I receive a “please wait” message, and I never get redirected. How can I download the form?

FDA 52

FDA Clinical Trials Licensing Licensing 52

The Pharma Data

JANUARY 27, 2021

technology platform simultaneously identifies both targets and the antibodies that bind to them, generating many promising new drug candidates to fuel the Company’s own clinical development pipeline or for additional licensing and partnering. View original content to download multimedia: [link].

Pharmaceuticals 52

Pharmaceuticals Clinical Trials Licensing Licensing 52

The Pharma Data

JANUARY 13, 2021

A preprint supporting Brilacidin’s COVID-19 treatment potential can be downloaded at the link below. Brilacidin for UP/UPS was licensed to Alfasigma S.p.A. Global COVID-19 Cases and Mortality An online tool tracking COVID-19 cases and mortality, both in the U.S.

Clinical Trials 52

Clinical Trials Trials Treatment Pharmaceuticals 52

The Pharma Data

OCTOBER 26, 2020

AR-711 is an in-licensed mAb that is directed against the receptor binding domain of the SARS-Cov 2 virus. AR-201 is a fully human IgG1 mAb out-licensed preclinical program aimed at neutralizing diverse clinical isolates of respiratory syncytial virus (RSV). View original content to download multimedia: [link]. Source link.

Pharmaceuticals 52

Pharmaceuticals Virus Hospitals Clinical Trials 52

The Pharma Data

JANUARY 22, 2021

iosBio , a UK-based biotechnology company, has announced an exclusive worldwide licensing agreement with ImmunityBio , a clinical-stage immunotherapy company, for rights to use iosBio’s OraPro vaccine platform technology to test the oral administration of ImmunityBio’s vaccine candidate. Download this exclusive report here.

Vaccine 52

Vaccine Immune Response Government RNA 52

The Pharma Data

JANUARY 26, 2021

The project portfolio is a combination of fully funded projects run in partnership with global pharmaceutical companies and innovative in-house projects with significant market and out-licensing potential. The following files are available for download: View original content: [link].

Disease 40

Disease Pharmaceutical Companies Treatment Licensing 40

PPD

JULY 9, 2024

Biotech and biopharma companies, however, must do all of this in the face of wildly fluctuating workloads — particularly during the post-marketing phase. At present, we have 99% first-cycle approvals, 100% licenses obtained, 100% dossiers validated and over 99% of submission milestones achieved on behalf of our clients. Let’s connect.

Compliance 52

Compliance Production Clinical Research Marketing 52

The Pharma Data

NOVEMBER 26, 2020

Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) date for review of the Company’s Biologics License Application (BLA) seeking accelerated approval of pegunigalsidase alfa (PRX–102) for the proposed treatment of adult patients with Fabry disease. Protalix has licensed to Pfizer Inc.

Disease 52

Disease Treatment Clinical Trials FDA 52

The Pharma Data

DECEMBER 29, 2020

is a medical device company with a novel and proprietary platform technology licensed from The University of Texas on behalf of MD Anderson Cancer Center. The Company is based in Houston, Texas , and is actively engaged in bringing the Rapid Acoustic Pulse (“RAP”) device to the market. About Soliton, Inc.

FDA 52

FDA Licensing Licensing Production 52

The Pharma Data

JANUARY 10, 2021

Download the slideshow of meetings on the Company website, in the Documentation section dedicated to investors: www.valbiotis.com/en/documents/. Its products are intended to be licensed to players in the health sector. Its products are intended to be licensed to players in the health sector.

International 40

International Pharmaceutical Companies Disease Licensing 40

The Pharma Data

NOVEMBER 24, 2020

Rolling Review, which means that a drug company can submit completed sections of its Biologic License Application (BLA) or New Drug Application (NDA) for review by FDA, rather than waiting until every section of the NDA is completed before the entire application can be reviewed. This information was brought to you by Cision [link].

FDA 40

FDA Clinical Trials Drugs Therapies 40

The Pharma Data

OCTOBER 19, 2020

The designation provides Berubicin with certain benefits during the product’s development to treat malignant gliomas and provides CNS with the potential for market exclusivity upon the drug’s approval for that use. View original content to download multimedia: [link]. .

Clinical Trials 52

Clinical Trials Trials Pharmaceuticals Treatment 52

The Pharma Data

JANUARY 13, 2021

View original content to download multimedia: [link]. MindMed does not undertake any obligation to update publicly any forward-looking statement. Media Contact: mindmed@150bond.com. . . SOURCE Mind Medicine (MindMed) Inc. .

Clinical Trials 52

Clinical Trials FDA Trials Production 52

The Pharma Data

JANUARY 31, 2021

is a medical device company with a novel and proprietary platform technology licensed from The University of Texas on behalf of MD Anderson Cancer Center. The Company is based in Houston, Texas , and is actively engaged in bringing the Rapid Acoustic Pulse (“RAP”) device to the market. About Soliton, Inc.

FDA 52

FDA Treatment Clinical Trials Licensing 52

The Pharma Data

JANUARY 10, 2021

During the fourth quarter of 2020, pricing for Idefirix ® was published in the first markets and agreements around reimbursement with healthcare providers and payers are expected to be completed in the early launch countries throughout the course of 2021. The following files are available for download: View original content: [link].

Therapies 40

Therapies Treatment Trials Disease 40

The Pharma Data

NOVEMBER 10, 2020

The company is listed on Nasdaq First North Premier Growth Market and is developing several parallel drug candidates based on three research platforms: NeuroRestore ® , Alzstatin ® and Painless. The following files are available for download: . About Alzstatin.

Pharmaceutical Companies 40

Pharmaceutical Companies Disease Treatment Pharmaceuticals 40

The Pharma Data

JANUARY 18, 2021

In-licensed from Merck KGaA, Darmstadt, Germany , atacicept has been studied previously in autoimmune diseases and shown to reduce autoantibodies in a dose-dependent fashion with once-weekly subcutaneous dosing and has a well-established and acceptable clinical safety profile. .” View original content to download multimedia: [link].

Disease 40

Disease Science Clinical Development Treatment 40

The Pharma Data

SEPTEMBER 16, 2020

The length of time that it takes for us to complete clinical trials and obtain regulatory approval for product marketing has in the past varied and we expect similar variability in the future. We develop product candidates internally and through licensing collaborations, partnerships and joint ventures. SOURCE Amgen. Source link.

Clinical Trials 52

Clinical Trials Production Trials Government 52

The Pharma Data

NOVEMBER 2, 2020

This acceptance by the FDA marks the first marketing application accepted for a treatment for achondroplasia in the United States. This information was included in the marketing application. BioMarin previously announced that the European Medicines Agency (EMA) validated the Company’s Marketing Authorization Application.

Drugs 40

Drugs FDA Treatment Pharmaceuticals 40

The Pharma Data

SEPTEMBER 20, 2020

The length of time that it takes for us to complete clinical trials and obtain regulatory approval for product marketing has in the past varied and we expect similar variability in the future. We develop product candidates internally and through licensing collaborations, partnerships and joint ventures. 2019;38:2953-2966. 2016;33:32.

Clinical Trials 52

Clinical Trials Production Trials Government 52

The Pharma Data

NOVEMBER 5, 2020

By a separate press release, the Company has today announced its intention to distribute the BUPI project to the shareholders of Moberg Pharma through a Lex Asea distribution with a subsequent listing on Nasdaq First North Growth Market during the Q1 of 2021. Other expenses for the Company’s operations.

Marketing 40

Marketing Production Regulations Pharma Companies 40

Nvidia Developer: Drug Discovery

MARCH 21, 2023

Descript’s AI-powered features and intuitive interface fuel YouTube and TikTok channels, top podcasts, and businesses using video for marketing, sales, and internal training and collaboration. WOMBO Dream, their main app has been downloaded more than 55M times and they average 3M images generated per day.

Engineering 52

Engineering Drugs Licensing Licensing 52

The Pharma Data

NOVEMBER 9, 2020

The length of time that it takes for Amgen to complete clinical trials and obtain regulatory approval for product marketing has in the past varied and Amgen expects similar variability in the future. Amgen develops product candidates internally and through licensing collaborations, partnerships and joint ventures. 2014; 133: 388–94.

Trials 52

Trials Production Clinical Trials Government 52

The Pharma Data

NOVEMBER 4, 2020

Please log on to the Concert website approximately 15 minutes prior to the scheduled webcast to ensure adequate time for any software downloads that may be required. License and research and development revenue. Unrealized gain (loss) on marketable equity securities.

Pharmaceuticals 52

Pharmaceuticals Clinical Trials Trials Treatment 52

The Pharma Data

DECEMBER 21, 2020

The length of time that it takes for Amgen to complete clinical trials and obtain regulatory approval for product marketing has in the past varied and Amgen expects similar variability in the future. Amgen develops product candidates internally and through licensing collaborations, partnerships and joint ventures. Available at: [link].

Trials 40

Trials Production Clinical Trials Therapies 40

Agency IQ

SEPTEMBER 29, 2023

The intent is to create a single market for data, establish common European data spaces, and allow the companies that generate the data to keep control and maintain trade secrets. market regardless of the location of the business. app interfaces) automatically and through bulk download where technically feasible.

Regulations 40

Regulations Government Production International 40

Drug Channels

FEBRUARY 22, 2022

Those who preorder will receive a download link before March 15. CLICK HERE to download a free pre-publication overview. As always, we have updated all market and industry data with the most current information available, including our annual analyses of the market positions of the largest pharmacies, specialty pharmacies, and PBMs.

Pharmacy 96

Pharmacy Specialty Pharmacies Biosimilars Licensing 96

Drug Channels

OCTOBER 10, 2023

I am pleased to announce our new 2023–24 Economic Report on Pharmaceutical Wholesalers and Specialty Distributors , available for purchase and immediate download. Click here to download a free report overview (including a summary of industry trends, the Table of Contents, and a List of Exhibits) New Drug Channels Institute Study: U.S.

Pharmaceuticals 40

Pharmaceuticals Specialty Pharmacies Pharmacy Biosimilars 40

Codon

FEBRUARY 13, 2024

Phage-based products have been licensed for use as antibacterial agents in the sanitation , food production , and animal health industries. Phages that can be essentially downloaded and synthesized by anyone, in any location, would solve those problems, he says. There is also a growing body of successful treatments in the U.S.,

Therapies 131

Therapies Virus DNA Clinical Trials 131

The Pharma Data

JANUARY 27, 2021

ZUBSOLV® stable and strong EBIT, despite challenging market due to COVID-19. Entered an exclusive license and supply agreement with Accord Healthcare for ZUBSOLV® covering 29 European countries. Entered an exclusive license and supply agreement with Accord Healthcare for ZUBSOLV® covering 29 European countries.

Therapies 40

Therapies Production Treatment FDA 40